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NCT06331312 · ClinicalTrials.gov registry record · Phase 3

Open-label, Long-term Safety Study of Secukinumab in Polymyalgia Rheumatica (PMR)

A Phase 3 study of Polymyalgia Rheumatica, sponsored by Novartis Pharmaceuticals.

Recruiting
Registry status
Phase 3
Development phase
288
Enrollment target
20
Study locations

NCT06331312 is a Phase 3 study of Polymyalgia Rheumatica that is actively recruiting participants, run by Novartis Pharmaceuticals. The registered enrollment target is 288 participants. The trial reports 20 study locations across 12 states.

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The verdict

NCT06331312, a Phase 3 study of Polymyalgia Rheumatica, is actively recruiting participants, sponsored by Novartis Pharmaceuticals.

RECRUITING
Registry status
Phase 3
Development phase
288 participants
Enrollment target
20
Study locations

Study Summary

The purpose of this extension study is to assess the safety and tolerability of secukinumab when administered long-term in patients with polymyalgia rheumatica.

Conditions Studied

Interventions

  • BIOLOGICAL Secukinumab

Study Locations (20)

Florida

  • Rheumatology Associates of South Florida - Boca Raton
  • UF Health Cancer Center - Gainesville
  • Sarasota Arthritis Res Ctr - Sarasota
  • West Broward Rheumatology Associates Inc - Tamarac

California

  • Orrin Troum MD and Medical Associates - Santa Monica
  • Center for Rheumatology Research - West Hills
  • Millennium Clinical Trials - Westlake Village

Texas

  • Prolato Clinical Research Center - Houston
  • Accurate Clinical Research Inc - San Antonio
  • Advanced Rheumatology of Houston - Spring

Arizona

  • Arizona Arthritis and Rheumatology Associates PLLC - Avondale
  • Sun Valley Arthritis Center Ltd - Peoria

Georgia

  • Arthritis Center of North Georgia - Gainesville

Maryland

  • Klein and Associates - Hagerstown

Massachusetts

  • Massachusetts General Hospital - Boston

Michigan

  • Clinical Research Inst of MI - Saint Clair Shores

Trial Details

FieldValue
Enrollment Target 288 participants
Start Date 2024-06-28
Est. Completion 2028-08-22
Phase Phase 3

Sponsor

Novartis Pharmaceuticals

1,375 total trials

What the Registry Record Tells You About NCT06331312

The ClinicalTrials.gov registry entry for NCT06331312 describes a study currently listed as recruiting, categorized as Phase 3. The registered enrollment target is 288 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Novartis Pharmaceuticals, which has 1,375 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Polymyalgia Rheumatica appearing as the primary indexed condition, and to 1 intervention - of which Secukinumab is the first listed.

NCT06331312 reports 20 study locations spanning 12 distinct geographic areas - top geographies include Florida, California, Texas.

Frequently Asked Questions

What is clinical trial NCT06331312 about?

NCT06331312 is a clinical study titled "Open-label, Long-term Safety Study of Secukinumab in Polymyalgia Rheumatica (PMR)". The purpose of this extension study is to assess the safety and tolerability of secukinumab when administered long-term in patients with polymyalgia rheumatica.

What is the current status of trial NCT06331312?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 288 participants. The study started on 2024-06-28. Estimated completion is 2028-08-22.

What conditions does trial NCT06331312 study?

This clinical trial studies the following conditions: Polymyalgia Rheumatica.

What interventions are being tested in trial NCT06331312?

The interventions under investigation include: Secukinumab (BIOLOGICAL).

Who is sponsoring clinical trial NCT06331312?

This trial is sponsored by Novartis Pharmaceuticals, which has 1,375 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06331312 being conducted?

This trial has 20 study locations across Arizona, California, Florida, Georgia, Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.